Electric sector time-of-flight mass spectrometer with adjustable ion optical elements
a mass spectrometer and time-of-flight technology, applied in the field of chemical and biochemical analysis, can solve the problems of reducing the accuracy, sensitivity and resolution of the mass spectrum, and the difficulty of achieving the optimal conditions of using a tof mass spectrometer, and achieve the problem of difficult to accurately determine the ionic mass in the mass spectrum
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example 1
Spectral Range (IgG)
[0107] The mass spectrometer of the present invention provides well-defined signals over a large spectral range. Spectral range is a characteristic of the mass spectrum and refers to the spectrometer's ability to detect and measure a broad range of masses from a given sample within a single spectrum. Ions outside the spectral range are usually not detectable and hence do not appear on the mass spectrum. Therefore, a spectrometer that provides a mass spectrum with a large mass range of interest may allow detection and measurement of a larger number of ions than one with a smaller spectral range.
[0108] To demonstrate the spectral range of the present invention, the apparatus of Embodiment A was used to obtain a TOF mass spectrum of IgG in a sinapinic acid (“SPA”) matrix on a gold chip. The sample was ionized by delayed extraction laser desorption ionization and the ions were detected with a sampling rate of 250 MHz. Referring toFIGS. 6A-6C, three portions of the ...
example 2
Spectral Range and Sensitivity (Peptide)
[0109] This experiment was performed to determine the spectral range and sensitivity of the apparatus with a peptide sample. In a manner similar to that described in Example 1, a tryptic digest of 100 fmole of bovine serum albumin (“BSA”) was prepared on a SEND-C18 chip (Ciphergen Biosystems™) and a mass spectrum was obtained. Referring to FIG. 7A-7H, eight portions from the single mass spectrum obtained are shown. The measured masses and resolutions of the peaks indicated are listed in Table 4 below. This experiment demonstrates that the masses of individual peptides may be obtained with high accuracy and resolution as measured in a single mass spectrum.
TABLE 4Selected Peptide Masses and ResolutionPeakMassResolution1545.33415602572.32314603922.46731804927.464239051399.7392061419.76399071795.85529082019.96540092458.196710103038.27530113511.578540
[0110] In order to determine the sensitivity of the apparatus, the experiment was repeated with ...
example 3
Mass Accuracy
[0111] To determine the mass accuracy of the present invention, the mass spectra of eight samples of a peptide mixture were acquired using the mass spectrometer of Embodiment A. All eight samples were introduced on a single gold chip in a cyanohydroxycinnamic acid (“CHCA”) matrix. The numbers listed in Table 6 were calculated from the corresponding peptide signals measured by these mass spectra As shown below, accurate masses for all five peptides were obtained using the Embodiment A mass spectrometer apparatus.
TABLE 6TOF Mass Spectra of Peptide Mixture (8 measurements)InsulinInsulinArg8-VasopressinSomatostatinDynorphin Aβ-chainαβ-chainsTrue Mass1083.4381636.7172146.1913493.6445807.653Average Mass1083.4051636.7002146.1923493.5695806.877SD (ppm)37.332.126.226.557.9Range (ppm)116.2103.080.772.8155.3Avg. Err. (ppm)40.123.718.926.6133.7Avg.-True (ppm)−30.110.20.1−21.3−133.7TOF Avg. (μsec)45.844756.312964.464282.2101105.9537TOF SD (ppm)18.616.013.113.228.9
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